Xavier Waltz

发表

Effects of exercise on markers of oxidative stress: an Ancillary analysis of the Alberta Physical Activity and Breast Cancer Prevention Trial

C. Friedenreich, K. Courneya, D. Brenner, 2016, BMJ Open Sport & Exercise Medicine.

Effects of hydroxyurea on blood rheology in sickle cell anemia: A two-years follow-up study.

K. Charlot, P. Connes, M. Etienne‐Julan, 2017, Clinical hemorheology and microcirculation.

Hemorheological alterations, decreased cerebral microvascular oxygenation and cerebral vasomotion compensation in sickle cell patients

A. Pichon, O. Hue, S. Sinnapah, 2012, American journal of hematology.

Haemolysis and abnormal haemorheology in sickle cell anaemia

O. Hue, S. Ballas, P. Connes, 2014, British journal of haematology.

Impaired oxygen uptake efficiency slope and off-transient kinetics of pulmonary oxygen uptake in sickle cell anemia are associated with hemorheological abnormalities.

K. Charlot, O. Hue, S. Sinnapah, 2015, Clinical hemorheology and microcirculation.

Hematological and hemorheological Determinants of the Six-Minute Walk Test Performance in Children with Sickle Cell Anemia

O. Hue, P. Connes, B. Tressières, 2013, PloS one.

Hydroxyurea treatment does not increase blood viscosity and improves red blood cell rheology in sickle cell anemia

K. Charlot, Ketty Lee, S. Ballas, 2015, Haematologica.

Effects of oxidative stress on red blood cell rheology in sickle cell patients

P. Connes, M. Romana, M. Hardy-Dessources, 2014, British journal of haematology.

Effects of Hydration Level and Heat Stress on Thermoregulatory Responses, Hematological and Blood Rheological Properties in Growing Pigs

D. Renaudeau, P. Connes, B. Bocage, 2014, PloS one.

Does increased red blood cell deformability raise the risk for osteonecrosis in sickle cell anemia?

P. Connes, M. Mukisi-Mukaza, B. Tressières, 2013, Blood.

Blood viscosity and hemodynamics during exercise.

A. Pichon, M. Simmonds, P. Connes, 2012, Clinical hemorheology and microcirculation.

Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell disease

R. Machado, P. Connes, B. Tressières, 2013, Haematologica.

Association between relative systemic hypertension and otologic disorders in patients with sickle cell‐hemoglobin C disorder

P. Connes, F. Lionnet, B. Tressières, 2014, American journal of hematology.

Pathophysiology and physical activity in patients with sickle cell anemia

P. Connes, Xavier Waltz, 2014 .

Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Study

V. Pialoux, Y. Bertrand, P. Joly, 2016, PloS one.

Relationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease.

P. Connes, B. Tressières, M. Etienne‐Julan, 2014, Clinical hemorheology and microcirculation.

Rheology of red blood cells in patients with HbC disease.

M. Billaud, P. Connes, M. Etienne‐Julan, 2016, Clinical hemorheology and microcirculation.

Blood Thixotropy in Patients with Sickle Cell Anaemia: Role of Haematocrit and Red Blood Cell Rheological Properties

M. Billaud, P. Connes, M. Etienne‐Julan, 2014, PloS one.

Delayed beneficial effect of acute exercise on red blood cell aggregate strength in patients with sickle cell anemia.

O. Hue, S. Sinnapah, P. Connes, 2012, Clinical hemorheology and microcirculation.

Hemorheological risk factors of acute chest syndrome and painful vaso-occlusive crisis in children with sickle cell disease

P. Connes, B. Tressières, M. Etienne‐Julan, 2012, Haematologica.

Male Gender, Increased Blood Viscosity, Body Mass Index and Triglyceride Levels Are Independently Associated with Systemic Relative Hypertension in Sickle Cell Anemia

P. Connes, B. Tressières, M. Etienne‐Julan, 2013, PloS one.

Overweight explains the increased red blood cell aggregation in patients with obstructive sleep apnea.

S. Sinnapah, P. Connes, Y. Lamarre, 2015, Clinical hemorheology and microcirculation.

Physical activity level is not a determinant of autonomic nervous system activity and clinical severity in children/adolescents with sickle cell anemia: A pilot study

K. Charlot, A. Pichon, O. Hue, 2015, Pediatric blood & cancer.

Acute Moderate Exercise Does Not Further Alter the Autonomic Nervous System Activity in Patients with Sickle Cell Anemia

K. Charlot, J. Barthélémy, O. Hue, 2014, PloS one.

Severe proliferative retinopathy is associated with blood hyperviscosity in sickle cell hemoglobin-C disease but not in sickle cell anemia.

P. Connes, S. Chahed, B. Tressières, 2013, Clinical hemorheology and microcirculation.

Which side of the balance determines the frequency of vaso-occlusive crises in children with sickle cell anemia: Blood viscosity or microvascular dysfunction?

K. Charlot, O. Hue, P. Connes, 2016, Blood cells, molecules & diseases.

Normal Muscle Oxygen Consumption and Fatigability in Sickle Cell Patients Despite Reduced Microvascular Oxygenation and Hemorheological Abnormalities

A. Pichon, O. Hue, P. Connes, 2012, PloS one.

Indirect viscosimetric method is less accurate than ektacytometry for the measurement of red blood cell deformability.

A. Pichon, P. Connes, M. Romana, 2015, Clinical hemorheology and microcirculation.

Cerebral and muscle microvascular oxygenation in children with sickle cell disease: Influence of hematology, hemorheology and vasomotion.

K. Charlot, O. Hue, P. Connes, 2017, Blood cells, molecules & diseases.

Effect of heat stress on blood rheology in different pigs breeds.

D. Renaudeau, P. Connes, J. Gourdine, 2014, Clinical hemorheology and microcirculation.

Decreased Hematocrit-To-Viscosity Ratio and Increased Lactate Dehydrogenase Level in Patients with Sickle Cell Anemia and Recurrent Leg Ulcers

P. Connes, M. Mukisi-Mukaza, B. Tressières, 2013, PloS one.

Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C disease

P. Connes, F. Lionnet, B. Tressières, 2014, Haematologica.

Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell disease

R. Machado, P. Connes, B. Tressières, 2013, Haematologica.

Alpha thalassemia protects sickle cell anemia patients from macro-albuminuria through its effects on red blood cell rheological properties.

P. Connes, B. Tressières, M. Etienne‐Julan, 2014, Clinical hemorheology and microcirculation.

Is there a relationship between the hematocrit-to-viscosity ratio and microvascular oxygenation in brain and muscle?

O. Hue, P. Connes, B. Tressières, 2015, Clinical hemorheology and microcirculation.

Does increased red blood cell deformability raise the risk for osteonecrosis in sickle cell anemia?

P. Connes, M. Mukisi-Mukaza, B. Tressières, 2013, Blood.